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In vitro activities of ketolide HMR 3647, macrolides, and clindamycin against coryneform bacteria

dc.creatorMartínez Martínez, Luises
dc.creatorPascual Hernández, Álvaroes
dc.creatorSuárez, Ana Isabeles
dc.creatorPerea Pérez, Evelio Josées
dc.date.accessioned2017-10-04T17:03:07Z
dc.date.available2017-10-04T17:03:07Z
dc.date.issued1998-12-01
dc.identifier.citationMartínez Martínez, L., Pascual Hernández, Á., Suárez, A.I. y Perea Pérez, E.J. (1998). In vitro activities of ketolide HMR 3647, macrolides, and clindamycin against coryneform bacteria. Antimicrobial Agents and Chemotherapy, 42 (12), 3290-3292.
dc.identifier.issn0066-4804 (impreso)es
dc.identifier.issn1098-6596 (electrónico)es
dc.identifier.urihttp://hdl.handle.net/11441/65014
dc.description.abstractThe in vitro activity of ketolide HMR 3647 against coryneform bacteria isolated from clinical samples was evaluated. Except against Corynebacterium jeikeium and C. urealyticum, HMR 3647 showed high activity against Corynebacterium spp., being more active than 14- and 16-membered macrolides, azithromycin, or clindamycin. HMR 3647 also had high in vitro activity against Brevibacterium spp. and Listeria monocytogenes.es
dc.formatapplication/pdfes
dc.language.isoenges
dc.publisherAmerican Society for Microbiologyes
dc.relation.ispartofAntimicrobial Agents and Chemotherapy, 42 (12), 3290-3292.
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleIn vitro activities of ketolide HMR 3647, macrolides, and clindamycin against coryneform bacteriaes
dc.typeinfo:eu-repo/semantics/articlees
dcterms.identifierhttps://ror.org/03yxnpp24
dc.type.versioninfo:eu-repo/semantics/publishedVersiones
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.contributor.affiliationUniversidad de Sevilla. Departamento de Microbiologíaes
idus.format.extent3 p.es
dc.journaltitleAntimicrobial Agents and Chemotherapyes
dc.publication.volumen42es
dc.publication.issue12es
dc.publication.initialPage3290es
dc.publication.endPage3292es

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